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<http://rdf.disgenet.org/nanopublications.trig#NP459224.RA-w0-9ltYoXw3mvem_z1NsL-ULn7kjus2qyeZUvcKXHo130_assertion> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://www.nanopub.org/nschema#Assertion> <http://rdf.disgenet.org/nanopublications.trig#NP459224.RA-w0-9ltYoXw3mvem_z1NsL-ULn7kjus2qyeZUvcKXHo130_head> .
<http://rdf.disgenet.org/nanopublications.trig#NP459224.RA-w0-9ltYoXw3mvem_z1NsL-ULn7kjus2qyeZUvcKXHo130_provenance> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://www.nanopub.org/nschema#Provenance> <http://rdf.disgenet.org/nanopublications.trig#NP459224.RA-w0-9ltYoXw3mvem_z1NsL-ULn7kjus2qyeZUvcKXHo130_head> .
<http://rdf.disgenet.org/nanopublications.trig#NP459224.RA-w0-9ltYoXw3mvem_z1NsL-ULn7kjus2qyeZUvcKXHo130_publicationInfo> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://www.nanopub.org/nschema#PublicationInfo> <http://rdf.disgenet.org/nanopublications.trig#NP459224.RA-w0-9ltYoXw3mvem_z1NsL-ULn7kjus2qyeZUvcKXHo130_head> .
<http://identifiers.org/ncbigene/5660> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C16612> <http://rdf.disgenet.org/nanopublications.trig#NP459224.RA-w0-9ltYoXw3mvem_z1NsL-ULn7kjus2qyeZUvcKXHo130_assertion> .
<http://linkedlifedata.com/resource/umls/id/C0745103> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C7057> <http://rdf.disgenet.org/nanopublications.trig#NP459224.RA-w0-9ltYoXw3mvem_z1NsL-ULn7kjus2qyeZUvcKXHo130_assertion> .
<http://rdf.disgenet.org/gene-disease-association.ttl#DGNacb7e162ce30575c9f9be0cc4aba78a0> <http://semanticscience.org/resource/SIO_000628> <http://identifiers.org/ncbigene/5660> <http://rdf.disgenet.org/nanopublications.trig#NP459224.RA-w0-9ltYoXw3mvem_z1NsL-ULn7kjus2qyeZUvcKXHo130_assertion> .
<http://rdf.disgenet.org/gene-disease-association.ttl#DGNacb7e162ce30575c9f9be0cc4aba78a0> <http://semanticscience.org/resource/SIO_000628> <http://linkedlifedata.com/resource/umls/id/C0745103> <http://rdf.disgenet.org/nanopublications.trig#NP459224.RA-w0-9ltYoXw3mvem_z1NsL-ULn7kjus2qyeZUvcKXHo130_assertion> .
<http://rdf.disgenet.org/gene-disease-association.ttl#DGNacb7e162ce30575c9f9be0cc4aba78a0> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://semanticscience.org/resource/SIO_001121> <http://rdf.disgenet.org/nanopublications.trig#NP459224.RA-w0-9ltYoXw3mvem_z1NsL-ULn7kjus2qyeZUvcKXHo130_assertion> .
<http://rdf.disgenet.org/nanopublications.trig#NP459224.RA-w0-9ltYoXw3mvem_z1NsL-ULn7kjus2qyeZUvcKXHo130_assertion> <http://purl.org/dc/terms/description> "[To understand the molecular mechanism(s) by which such mutations cause FHC, we analyzed (i) the accumulation of human cMyBP-C mutants in fetal rat cardiomyocytes, and (ii) the protein sequence of the human wild-type (wt) cMyBP-C by hydrophobic cluster analysis with the aim of identifying new putative myosin-binding site(s).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en <http://rdf.disgenet.org/nanopublications.trig#NP459224.RA-w0-9ltYoXw3mvem_z1NsL-ULn7kjus2qyeZUvcKXHo130_provenance> .
<http://rdf.disgenet.org/nanopublications.trig#NP459224.RA-w0-9ltYoXw3mvem_z1NsL-ULn7kjus2qyeZUvcKXHo130_assertion> <http://purl.org/ontology/wi/core#evidence> <http://rdf.disgenet.org/v2.1.0/void.ttl#source_evidence_literature> <http://rdf.disgenet.org/nanopublications.trig#NP459224.RA-w0-9ltYoXw3mvem_z1NsL-ULn7kjus2qyeZUvcKXHo130_provenance> .
<http://rdf.disgenet.org/nanopublications.trig#NP459224.RA-w0-9ltYoXw3mvem_z1NsL-ULn7kjus2qyeZUvcKXHo130_assertion> <http://semanticscience.org/resource/SIO_000772> <http://identifiers.org/pubmed/10610770> <http://rdf.disgenet.org/nanopublications.trig#NP459224.RA-w0-9ltYoXw3mvem_z1NsL-ULn7kjus2qyeZUvcKXHo130_provenance> .
<http://rdf.disgenet.org/nanopublications.trig#NP459224.RA-w0-9ltYoXw3mvem_z1NsL-ULn7kjus2qyeZUvcKXHo130_assertion> <http://www.w3.org/ns/prov#wasDerivedFrom> <http://rdf.disgenet.org/v2.1.0/void.ttl#befree-20140225> <http://rdf.disgenet.org/nanopublications.trig#NP459224.RA-w0-9ltYoXw3mvem_z1NsL-ULn7kjus2qyeZUvcKXHo130_provenance> .
<http://rdf.disgenet.org/nanopublications.trig#NP459224.RA-w0-9ltYoXw3mvem_z1NsL-ULn7kjus2qyeZUvcKXHo130_assertion> <http://www.w3.org/ns/prov#wasGeneratedBy> <http://purl.obolibrary.org/obo/eco.owl#ECO_0000203> <http://rdf.disgenet.org/nanopublications.trig#NP459224.RA-w0-9ltYoXw3mvem_z1NsL-ULn7kjus2qyeZUvcKXHo130_provenance> .
<http://rdf.disgenet.org/v2.1.0/void.ttl#befree-20140225> <http://purl.org/pav/2.0/importedOn> "2014-02-25"^^<http://www.w3.org/2001/XMLSchema#date> <http://rdf.disgenet.org/nanopublications.trig#NP459224.RA-w0-9ltYoXw3mvem_z1NsL-ULn7kjus2qyeZUvcKXHo130_provenance> .
<http://rdf.disgenet.org/v2.1.0/void.ttl#source_evidence_literature> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://purl.obolibrary.org/obo/eco.owl#ECO_0000212> <http://rdf.disgenet.org/nanopublications.trig#NP459224.RA-w0-9ltYoXw3mvem_z1NsL-ULn7kjus2qyeZUvcKXHo130_provenance> .
<http://rdf.disgenet.org/v2.1.0/void.ttl#source_evidence_literature> <http://www.w3.org/2000/01/rdf-schema#comment> "Gene-disease associations inferred from text-mining the literature."@en <http://rdf.disgenet.org/nanopublications.trig#NP459224.RA-w0-9ltYoXw3mvem_z1NsL-ULn7kjus2qyeZUvcKXHo130_provenance> .
<http://rdf.disgenet.org/v2.1.0/void.ttl#source_evidence_literature> <http://www.w3.org/2000/01/rdf-schema#label> "DisGeNET evidence - LITERATURE"@en <http://rdf.disgenet.org/nanopublications.trig#NP459224.RA-w0-9ltYoXw3mvem_z1NsL-ULn7kjus2qyeZUvcKXHo130_provenance> .
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